3,4-dichlorofluorobenzene
Conditions | Yield |
---|---|
With lithium hydroxide monohydrate; silver trifluoromethanesulfonate; Selectfluor In ethyl acetate at 55℃; Sealed tube; | 75% |
4-bromo-1,2-dichlorobenzene
3,4-dichlorofluorobenzene
Conditions | Yield |
---|---|
Stage #1: 4-bromo-1,2-dichlorobenzene With TurboGrignard In tetrahydrofuran; 1,4-dioxane at 0 - 25℃; Inert atmosphere; Stage #2: With N-fluorobis(benzenesulfon)imide In dichloromethane; octadecafluorodecahydronaphthalene (cis+trans) at -78 - 20℃; Inert atmosphere; | 34% |
Stage #1: 4-bromo-1,2-dichlorobenzene With TurboGrignard In tetrahydrofuran at 0℃; Inert atmosphere; Stage #2: With N-fluorobis(benzenesulfon)imide In dichloromethane; octadecafluorodecahydronaphthalene (cis+trans) at -78 - 25℃; Inert atmosphere; | 34% |
Conditions | Yield |
---|---|
Reaktion nach Sandmeyer; |
Conditions | Yield |
---|---|
With hydrogenchloride; tetrafluoroboric acid; sodium nitrite Erhitzen des Reaktionsprodukts auf 150grad; |
2,3-dichlorofluorobenzene
A
3,4-dichlorofluorobenzene
B
3-chlorofluorobenzene
C
1,4-dichloro-2-fluorobenzene
D
1,3-dichloro-4-fluorobenzene
Conditions | Yield |
---|---|
In acetonitrile for 10h; Product distribution; Irradiation; | A 5 % Chromat. B 5 % Chromat. C 13 % Chromat. D 1 % Chromat. |
sulfuric acid
m,p-dichloroaniline
A
3,4-dichlorofluorobenzene
B
3,4-dichlorophenol
C
1,2-dichloro-benzene
Conditions | Yield |
---|---|
Behandeln der Diazoloesung mit heisser Flusssaeure.Diazotization; |
fluorobenzene
A
3,4-dichlorofluorobenzene
B
1-Chloro-4-fluorobenzene
C
1,3-dichloro-4-fluorobenzene
Conditions | Yield |
---|---|
Einleiten von 2 Mol Chlor; |
3,4-dichlorofluorobenzene
3,4-dichlorofluorobenzene
Conditions | Yield |
---|---|
With tetrakis(acetonitrile)copper(I)tetrafluoroborate; [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate; cesium fluoride In acetone at 30℃; for 20h; Inert atmosphere; Irradiation; | 63 %Spectr. |
3,4-dichlorofluorobenzene
N,N-dimethyl-formamide
2,3-Dichloro-6-fluorobenzaldehyde
Conditions | Yield |
---|---|
Stage #1: 3,4-dichlorofluorobenzene With lithium diisopropyl amide In tetrahydrofuran at -65℃; for 0.5h; Inert atmosphere; Stage #2: N,N-dimethyl-formamide In tetrahydrofuran at -65℃; for 0.333333h; Inert atmosphere; | 94% |
Conditions | Yield |
---|---|
With 1,2-bis(N-methylimidazolium)ethane chloroaluminate at 60℃; for 4h; Time; | 92.9% |
chloro-trimethyl-silane
3,4-dichlorofluorobenzene
1-fluoro-3,4-bis(trimethylsilyl)benzene
Conditions | Yield |
---|---|
With 1,3-dimethyl-2-imidazolidinone; magnesium; copper(l) chloride; lithium chloride at 55℃; for 17h; | 88% |
Conditions | Yield |
---|---|
Stage #1: 2,2,6,6-tetramethylpiperidin-1-ol; 3,4-dichlorofluorobenzene With potassium tert-butylate In tetrahydrofuran at 20℃; for 4h; Stage #2: With hydrogenchloride In diethyl ether for 0.166667h; Product distribution / selectivity; | 84% |
3,4-dichlorofluorobenzene
3-Bromonitrobenzene
2,3-dichloro-6-fluoro-3’-nitrobiphenyl
Conditions | Yield |
---|---|
With PdCl(1,4-bis(diphenylphosphino)butane)(C3H5); potassium pivalate In N,N-dimethyl acetamide at 150℃; for 16h; Inert atmosphere; regioselective reaction; | 64% |
3,4-dichlorofluorobenzene
1,3-Diamino-2-hydroxypropane
2-(3,4-dichlorophenoxy)propane-1,3-diamine
Conditions | Yield |
---|---|
Stage #1: 1,3-Diamino-2-hydroxypropane With sodium hydride In N,N-dimethyl acetamide Stage #2: 3,4-dichlorofluorobenzene In N,N-dimethyl acetamide at 170℃; for 0.0694444h; microwave irradiation; | 62% |
3,5-dimethoxyphenol
3,4-dichlorofluorobenzene
1,2-dichloro-4-(3,5-dimethoxyphenoxy)benzene
Conditions | Yield |
---|---|
Stage #1: 3,5-dimethoxyphenol With caesium carbonate In 1-methyl-pyrrolidin-2-one at 50℃; for 0.5h; Inert atmosphere; Stage #2: 3,4-dichlorofluorobenzene In 1-methyl-pyrrolidin-2-one at 120℃; for 2h; Inert atmosphere; | 60% |
3-Bromopyridine
3,4-dichlorofluorobenzene
3-(2,3-dichloro-6-fluorophenyl)pyridine
Conditions | Yield |
---|---|
With PdCl(1,4-bis(diphenylphosphino)butane)(C3H5); potassium pivalate In N,N-dimethyl acetamide at 150℃; for 16h; Inert atmosphere; regioselective reaction; | 58% |
Conditions | Yield |
---|---|
With PdCl(1,4-bis(diphenylphosphino)butane)(C3H5); tetrabutylammomium bromide; potassium pivalate In N,N-dimethyl acetamide at 150℃; for 16h; Inert atmosphere; Green chemistry; regioselective reaction; | 39% |
Conditions | Yield |
---|---|
at 180℃; nach 7 Tagen; |
Conditions | Yield |
---|---|
With methanol at 180℃; | |
at 180℃; nach 6 Stunden; |
Conditions | Yield |
---|---|
With sodium methylate | |
With methanol; sodium methylate at 180℃; |
Conditions | Yield |
---|---|
With sulfuric acid; nitric acid |
3,4-dichlorofluorobenzene
1,2,4-Tribromo-5,6-dichloro-3-fluoro-benzene
Conditions | Yield |
---|---|
(i) Hg(O2CCF3)2, (ii) KBr3, aq. MeOH; Multistep reaction; |
3,4-dichlorofluorobenzene
4,5-dichloro-2-fluorobenzenesulfonyl chloride
Conditions | Yield |
---|---|
With chlorosulfonic acid |
3,4-dichlorofluorobenzene
4-(hydroxyphenylmethyl)piperidine-1-carboxylic acid tert-butyl ester
Conditions | Yield |
---|---|
Stage #1: 4-(hydroxyphenylmethyl)piperidine-1-carboxylic acid tert-butyl ester With sodium hydride In dimethyl sulfoxide at 20℃; Stage #2: 3,4-dichlorofluorobenzene With Potassium benzoate In dimethyl sulfoxide at 65℃; |
3,4-dichlorofluorobenzene
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1.1: NaH / N,N-dimethyl-acetamide 1.2: 62 percent / N,N-dimethyl-acetamide / 0.07 h / 170 °C / microwave irradiation 2.1: 53 percent / ethanol / 0.06 h / 140 °C / microwave irradiation 3.1: 95 percent / acetonitrile / 0.14 h / 130 °C / microwave irradiation 4.1: 100 percent / NH4OH / H2O / 0.14 h / 150 °C / microwave irradiation View Scheme |
3,4-dichlorofluorobenzene
5-(3,4-dichlorophenoxy)-3,4,5,6-tetrahydropyrimidine-2(1H)-thione
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: NaH / N,N-dimethyl-acetamide 1.2: 62 percent / N,N-dimethyl-acetamide / 0.07 h / 170 °C / microwave irradiation 2.1: 53 percent / ethanol / 0.06 h / 140 °C / microwave irradiation View Scheme |
3,4-dichlorofluorobenzene
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: NaH / N,N-dimethyl-acetamide 1.2: 62 percent / N,N-dimethyl-acetamide / 0.07 h / 170 °C / microwave irradiation 2.1: 53 percent / ethanol / 0.06 h / 140 °C / microwave irradiation 3.1: 95 percent / acetonitrile / 0.14 h / 130 °C / microwave irradiation View Scheme |
3,4-dichlorofluorobenzene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: NaH / N,N-dimethyl-acetamide 1.2: 62 percent / N,N-dimethyl-acetamide / 0.07 h / 170 °C / microwave irradiation 2.1: 53 percent / propan-2-ol / 0.17 h / 120 °C / microwave irradiation View Scheme |
The Benzene,1,2-dichloro-4-fluoro-, with CAS registry number 1435-49-0, belongs to the following product categories: (1)Chlorine Compounds; (2)Fluorine Compounds. It has the systematic name of 1,2-dichloro-4-fluorobenzene. This chemical is a kind of clear colorless to slightly yellow liquid. The main use of this chemical is for the intermediate of pesticide, medicine and liquid crystal material.
Physical properties of Benzene,1,2-dichloro-4-fluoro-: (1)ACD/LogP: 2.84; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 2.84; (4)ACD/LogD (pH 7.4): 2.84; (5)ACD/BCF (pH 5.5): 85.36; (6)ACD/BCF (pH 7.4): 85.36; (7)ACD/KOC (pH 5.5): 839.47; (8)ACD/KOC (pH 7.4): 839.47; (9)#H bond acceptors: 0; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 0; (12)Polar Surface Area: 0 Å2; (13)Index of Refraction: 1.525; (14)Molar Refractivity: 36.03 cm3; (15)Molar Volume: 117.5 cm3; (16)Polarizability: 14.28×10-24cm3; (17)Surface Tension: 35.1 dyne/cm; (18)Enthalpy of Vaporization: 39.18 kJ/mol; (19)Vapour Pressure: 1.79 mmHg at 25°C.
When you are using this chemical, please be cautious about it as the following:
The Benzene,1,2-dichloro-4-fluoro- irritates to eyes, respiratory system and skin. And this chemical is harmful if swallowed. When use it, wear suitable protective clothing, gloves and eye/face protection. If contact with eyes, rinse immediately with plenty of water and seek medical advice.
You can still convert the following datas into molecular structure:
(1)SMILES: Fc1cc(Cl)c(Cl)cc1
(2)InChI: InChI=1/C6H3Cl2F/c7-5-2-1-4(9)3-6(5)8/h1-3H
(3)InChIKey: QSDKXMVGRLVIQV-UHFFFAOYAG
(4)Std. InChI: InChI=1S/C6H3Cl2F/c7-5-2-1-4(9)3-6(5)8/h1-3H
(5)Std. InChIKey: QSDKXMVGRLVIQV-UHFFFAOYSA-N
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